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Structure of 96314-29-3
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This chiral pyrrolidine derivative features a tert-butoxycarbonyl-protected amine and a phenyl-substituted carbon center, enabling direct incorporation into peptide synthesis. The (2S,4S) stereochemistry ensures high diastereoselectivity in cyclization reactions, while the bench-stable Boc group simplifies handling and purification under standard conditions.
(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and peptidomimetics. The Boc-protected pyrrolidine scaffold exhibits excellent bench stability, facilitates straightforward deprotection under mild acidic conditions, and demonstrates broad compatibility with standard coupling reactions. Its phenyl-substituted ring enhances rigidity and provides a hydrophobic moiety suitable for medicinal chemistry optimization.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: